GlaxoSmithKline, Waltham, MA.
GlaxoSmithKline, Uxbridge, UK.
J Manag Care Spec Pharm. 2021 Oct;27(10):1377-1387. doi: 10.18553/jmcp.2021.27.10.1377.
Ovarian cancer (OC) is the fifth leading cause of cancer death in women and has the highest mortality rate of gynecological cancers. Niraparib was recently approved by the FDA for the maintenance treatment of adult patients with advanced epithelial OC in complete or partial response to first-line platinum-based chemotherapy (PBC) regardless of biomarker status. To estimate the direct economic impact on US payers of adding niraparib as a first-line maintenance therapy for patients with advanced OC. The model considered 2 scenarios: a current scenario in which niraparib does not have regulatory approval for first-line maintenance therapy and a future scenario in which niraparib has regulatory approval for first-line maintenance therapy. The budget impact was calculated as the difference in cost between the 2 scenarios. The budget impact model (BIM) considered 2 different US health care payer perspectives: a commercial health plan and a Medicare plan. Both payer perspectives were assumed to have a hypothetical 1 million affiliates that were covered. Epidemiological data was used to estimate the eligible incident population of patients with OC. Active surveillance, bevacizumab (as a monotherapy), and olaparib (as a monotherapy restricted to patients with the breast cancer gene [] mutation) were included in the model as alternative maintenance treatment options (maintenance treatment options required 1% market share for inclusion). Cost categories considered in the BIM included diagnostic testing, treatment acquisition and administration, treatment-emergent adverse events, and subsequent therapy. Results were presented as an incremental budget impact to payers over 3 years. For a commercial health plan of 1 million affiliates, the estimated impact of adding niraparib as a first-line maintenance treatment option for advanced epithelial OC was calculated as $87,906, $93,106, and $87,037 for years 1, 2, and 3, respectively. The average budget impact per member per month was $0.007. For a Medicare health plan of 1 million affiliates, the estimated impact was calculated as $206,785, $219,017, and $204,739 for years 1, 2, and 3, respectively. The average budget impact per member per month was $0.018. One-way sensitivity analyses suggested that budget impact was most sensitive to the treatment duration and market share of niraparib, the non-treatment-specific data on overall survival rates, and the treatment duration of bevacizumab. Treatment of drug-specific adverse events had little impact on the budget model. The model estimated a minimal budget impact to both a commercial or Medicare health plan following the introduction of niraparib as a first-line maintenance therapy for patients with advanced epithelial OC who are in complete or partial response to first-line PBC regardless of biomarker status. This study was financially supported by GlaxoSmithKline. Liu, Hawkes, Maiese, and Hurteau are employees of GlaxoSmithKline. Travers was employed by GlaxoSmithKline at the time of this study. Spalding and Walder are employees of FIECON Ltd., which was contracted by GlaxoSmithKline to develop the budget impact model used in this study.
卵巢癌(OC)是女性癌症死亡的第五大主要原因,也是妇科癌症中死亡率最高的癌症。尼拉帕利最近被 FDA 批准用于对一线含铂化疗(PBC)完全或部分缓解的晚期上皮性 OC 成年患者的维持治疗,无论生物标志物状态如何。为了估计将尼拉帕利作为晚期 OC 患者的一线维持治疗添加到美国支付者的直接经济影响。该模型考虑了 2 种情况:目前尼拉帕利没有一线维持治疗监管批准的情况,以及未来尼拉帕利具有一线维持治疗监管批准的情况。预算影响被计算为两种情况之间的成本差异。预算影响模型(BIM)考虑了 2 种不同的美国医疗保健支付者视角:商业健康计划和医疗保险计划。假设这两个支付者视角都有一个假设的 100 万受保人。使用流行病学数据估计 OC 患者的合格发病人口。主动监测、贝伐珠单抗(作为单药治疗)和奥拉帕利(作为仅适用于乳腺癌基因 []突变患者的单药治疗)被纳入模型作为替代维持治疗选择(维持治疗选择需要 1%的市场份额才能纳入)。BIM 中考虑的成本类别包括诊断测试、治疗获取和管理、治疗相关不良事件以及随后的治疗。结果以 3 年内支付者的增量预算影响呈现。对于 100 万会员的商业健康计划,添加尼拉帕利作为晚期上皮性 OC 一线维持治疗选择的估计影响分别为第 1、2 和第 3 年的 87906 美元、93106 美元和 87037 美元。每位会员每月的平均预算影响为 0.007 美元。对于 100 万会员的医疗保险计划,估计影响分别为第 1、2 和第 3 年的 206785 美元、219017 美元和 204739 美元。每位会员每月的平均预算影响为 0.018 美元。单向敏感性分析表明,预算影响对尼拉帕利的治疗持续时间和市场份额、总体生存率的非治疗特异性数据以及贝伐珠单抗的治疗持续时间最为敏感。药物特异性不良反应的治疗对预算模型影响不大。该模型估计,无论生物标志物状态如何,对于接受一线 PBC 完全或部分缓解的晚期上皮性 OC 患者,将尼拉帕利作为一线维持治疗药物引入后,商业或医疗保险健康计划的预算影响最小。本研究得到葛兰素史克公司的资助。刘、霍克茨、迈泽和赫特奥是葛兰素史克公司的员工。特雷弗斯在本研究期间受雇于葛兰素史克公司。斯波尔丁和沃尔德是 FIECON 有限公司的员工,该公司受雇于葛兰素史克公司开发本研究中使用的预算影响模型。